Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Anil, Vasudevan"'
Autor:
Eric R. Goedken, Maria A. Argiriadi, Justin D. Dietrich, Andrew M. Petros, Navasona Krishnan, Sanjay C. Panchal, Wei Qiu, Haihong Wu, Haizhong Zhu, Ashley M. Adams, Pierre M. Bodelle, Lucas Goguen, Paul L. Richardson, Peter F. Slivka, Myron Srikumaran, Anup K. Upadhyay, Bainan Wu, Russell A. Judge, Anil Vasudevan, Sujatha M. Gopalakrishnan, Philip B. Cox, Vincent S. Stoll, Chaohong Sun
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Anti-IL17A therapies have proven effective for numerous inflammatory diseases including psoriasis, axial spondylitis and psoriatic arthritis. Modulating and/or antagonizing protein–protein interactions of IL17A cytokine binding to its cell
Externí odkaz:
https://doaj.org/article/73a129f16e244becaaa09ce714e81a66
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background Congenital anomalies of the kidney and urinary tract (CAKUT) cover a spectrum of structural malformations that result from aberrant morphogenesis of kidney and urinary tract. It is the most prevalent cause of kidney failure in chi
Externí odkaz:
https://doaj.org/article/fb268c6a01974f0ab5e416ed7e3ebcfd
Autor:
Stuti Panigrahi, Varsha Chhotusing Pardeshi, Karthikeyan Chandrasekaran, Karthik Neelakandan, Hari PS, Anil Vasudevan
Publikováno v:
Clinical and Experimental Pediatrics, Vol 64, Iss 7, Pp 355-363 (2021)
Background Nephrotic syndrome (NS) is a common renal disorder in children attributed to podocyte injury. However, children with the same diagnosis have markedly variable treatment responses, clinical courses, and outcomes, suggesting molecular hetero
Externí odkaz:
https://doaj.org/article/0bd277734ae54ce6bc74ba8634d5868f
Autor:
Bilal M. Akhtar, Priyanka Bhatia, Shubhra Acharya, Sanjeev Sharma, Yojet Sharma, Aswathy Bhuvanendran Nair Suseela Devi, Kavina Ganapathy, Anil Vasudevan, Padinjat Raghu
Publikováno v:
Biology Open, Vol 11, Iss 1 (2022)
Human brain development is a complex process where multiple cellular and developmental events are coordinated to generate normal structure and function. Alteration in any of these events can impact brain development, manifesting clinically as neurode
Externí odkaz:
https://doaj.org/article/48ec128bd724416b9cef88b39392e524
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 2, Pp 334-338 (2019)
Seroconversion following hepatitis B vaccination is low in children with chronic kidney disease (CKD). This study aimed to assess the seroconversion and persistence of protective immunity following hepatitis B vaccination in children with CKD. This p
Externí odkaz:
https://doaj.org/article/fd3daebb54c24d2797dec92094206374
Autor:
Andrea G. Shergalis, Violeta L. Marin, David Y. Rhee, Sameera Senaweera, Rebecca L. McCloud, Judith A. Ronau, Charles W. Hutchins, Shaun McLoughlin, Kevin R. Woller, Scott E. Warder, Anil Vasudevan, Justin M. Reitsma
Publikováno v:
ACS Chemical Biology. 18:331-339
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21c19f36bf74a5e7cb655d9ba46e9868
https://doi.org/10.1021/acschembio.2c00747
https://doi.org/10.1021/acschembio.2c00747
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background Steroid resistant nephrotic syndrome (SRNS) is a genetically heterogeneous disease with significant phenotypic variability. More than 53 podocyte-expressed genes are implicated in SRNS which complicates the routine use of genetic
Externí odkaz:
https://doaj.org/article/f446e0df13e84d049bdb85f6a200b19c
Publikováno v:
CEN Case Rep
OHVIRA syndrome (or Herlyn-Werner-Wunderlich syndrome) is a rare condition, consisting classically of obstructed hemi-vagina with ipsilateral renal agenesis. It may be associated with complex uterine malformations and more rarely with lower urinary t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::688da4f104bcac0904ee4ea1da45b620
https://doi.org/10.1007/s13730-022-00754-7
https://doi.org/10.1007/s13730-022-00754-7
Publikováno v:
CEN Case Rep
Magnesium is one of the most abundant electrolytes in the human body but is often forgotten when it comes to the evaluation of an infant presenting with hypocalcemia. Its deficiency can present as neurological, cardiac and skeletal symptoms. Familial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0746c8b0af652bf692ba11876cc896cd
https://doi.org/10.1007/s13730-022-00734-x
https://doi.org/10.1007/s13730-022-00734-x
Autor:
Mamta Puraswani, Priyanka Khandelwal, Himanshi Saini, Savita Saini, Bahadur Singh Gurjar, Aditi Sinha, Rajashri Pramod Shende, Tushar Kanti Maiti, Abhishek Kumar Singh, Uma Kanga, Uma Ali, Indira Agarwal, Kanav Anand, Narayan Prasad, Padmaraj Rajendran, Rajiv Sinha, Anil Vasudevan, Anita Saxena, Sanjay Agarwal, Pankaj Hari, Arvind Sahu, Satyajit Rath, Arvind Bagga
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Background: Atypical hemolytic uremic syndrome (aHUS), an important cause of acute kidney injury (AKI), is characterized by dysregulation of the alternative complement pathway. Autoantibodies to factor H (FH), a chief regulator of this pathway, accou
Externí odkaz:
https://doaj.org/article/06c62aefba2147c6be52a9d372522328